Canonical Allele Identifier: CA150175987
Gene: ESR1 HGNC NCBI

Linked Data

dbSNP Id: rs56254212

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152101149T>G , CM000668.2:g.152101149T>G GRCh38
NC_000006.11:g.152422284T>G , CM000668.1:g.152422284T>G GRCh37
NC_000006.10:g.152463977T>G NCBI36
NG_008493.1:g.415654T>G
NG_008493.2:g.449459T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000206249.8:c.*2183T>G MANE Select ENSP00000206249.3:n.*2183T>G
ENST00000641399.1:n.1070+2229T>G
ENST00000206249.7:c.*2183T>G ENSP00000206249.3:n.*2183T>G
ENST00000427531.6:c.851-24117T>G ENSP00000394721.2:n.851-24117T>G
ENST00000440973.5:c.*2183T>G ENSP00000405330.1:n.*2183T>G
ENST00000443427.5:c.*2183T>G ENSP00000387500.1:n.*2183T>G
NM_000125.3:c.*2183T>G NP_000116.2:n.*2183T>G
NM_001122740.1:c.*2183T>G NP_001116212.1:n.*2183T>G
NM_001122741.1:c.*2183T>G NP_001116213.1:n.*2183T>G
NM_001122742.1:c.*2183T>G NP_001116214.1:n.*2183T>G
NM_001291230.1:c.*2183T>G NP_001278159.1:n.*2183T>G
NM_001291241.1:c.*2183T>G NP_001278170.1:n.*2183T>G
XM_006715374.2:c.*2386T>G XP_006715437.1:n.*2386T>G
XM_006715375.2:c.*2183T>G XP_006715438.1:n.*2183T>G
XM_011535543.1:c.*2183T>G XP_011533845.1:n.*2183T>G
XM_011535544.1:c.*2183T>G XP_011533846.1:n.*2183T>G
XM_011535545.1:c.*2183T>G XP_011533847.1:n.*2183T>G
XM_011535546.1:c.*2183T>G XP_011533848.1:n.*2183T>G
XM_011535548.1:c.*2183T>G XP_011533850.1:n.*2183T>G
XM_011535549.1:c.*2183T>G XP_011533851.1:n.*2183T>G
NM_001328100.1:c.851-24117T>G NP_001315029.1:n.851-24117T>G
XM_006715374.3:c.*2386T>G XP_006715437.1:n.*2386T>G
NM_000125.4:c.*2183T>G MANE Select NP_000116.2:n.*2183T>G
NM_001328100.2:c.851-24117T>G NP_001315029.1:n.851-24117T>G
NM_001122740.2:c.*2183T>G NP_001116212.1:n.*2183T>G
NM_001122741.2:c.*2183T>G NP_001116213.1:n.*2183T>G
NM_001122742.2:c.*2183T>G NP_001116214.1:n.*2183T>G
NM_001291230.2:c.*2183T>G NP_001278159.1:n.*2183T>G
NM_001291241.2:c.*2183T>G NP_001278170.1:n.*2183T>G
NM_001385568.1:c.*2183T>G NP_001372497.1:n.*2183T>G
NM_001385569.1:c.*2183T>G NP_001372498.1:n.*2183T>G
NM_001385570.1:c.*2386T>G NP_001372499.1:n.*2386T>G
NM_001385571.1:c.*2386T>G NP_001372500.1:n.*2386T>G
NM_001385572.1:c.*2386T>G NP_001372501.1:n.*2386T>G